Dizop Minoxidil Topical Gel

Manufacturer
Shenzhen Joyuflsh Technology Co.,Ltd.
Effective date
2024-04-23
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 00:11:21

Label at a glance#

ProductDizop Minoxidil Topical Gel
Active ingredientMINOXIDIL
Label structure13 sections

Storage and handling

Store between 41 and 86℉ (5 and 30 ℃). Avoid freezing and exposure to excessive heat above 95℉ (35°C)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Dizop Minoxidil Topical Gel

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

OTC - PURPOSE SECTION

Reactivates Hair Follicles To Stimulate RegrowthEasy-To-Use Minoxidil Gel

Minoxidil Topical Gel, 5% (For Men), is designed for men experiencing general hair
thinning on the top of the scalp, as depicted.

INDICATIONS & USAGE SECTION

Hair regrowth treatment for men.
Use to Regrow Hair on the Top of the Scalp (See Pictures on the Side of this Carton).

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Your degree of hair loss differs from that shown on the side of this carton because this product may not work for you.
Your hair loss is sudden, patchy, or a combination of both.
You are under 18 years of age. Please do not use it on babies or children.
Your scalp is red, inflamed, infected, irritated, or painful.
You use other medicines on the scalp.

OTC - WHEN USING SECTION

Do not use more than directed.
Avoid contact with the eyes, ears, and mouth. In the event of accidental contact withthe eyes, rinse the affected area with a generous amount of cool tap waterimmediately.
lt takes time to regrow hair. Results may occur after two months of once-daily useFor some individuals, it may take at least four months before results becomenoticeable.
The efficacy of this product in promoting hair regrowth can differ from person to person, and it may not work for every man.

OTC - STOP USE SECTION

Stop use and ask a doctor if you experience chest pain, a rapid heartbeat,faintness, or dizziness, or if scalp irritation or redness occurs. These may be signs of a serious condition

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222

DOSAGE & ADMINISTRATION SECTION

Apply 1 ml onto the scalp, where hair loss occurs, once daily and massaging gently for absorption.

STORAGE AND HANDLING SECTION

Store between 41 and 86℉ (5 and 30 ℃). Avoid freezing and exposure to excessive heat above 95℉ (35°C)

INACTIVE INGREDIENT SECTION

STEARIC ACID
OLEIC ACID
POLYSORBATE 80
SORBITAN MONOOLEATE
CARBOMER HOMOPOLYMER
GLYCERIN
PURIFIED WATER

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

43274327

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2668433minoxidil 5 % Topical GelPSN9
2668433minoxidil 0.05 MG/MG Topical GelSCD9
2668433minoxidil 5 % Topical GelSY9

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MINOXIDIL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83766-101-01Dizop Minoxidil Topical Gel100 mL in 1 BOTTLEGEL1009
83766-101-02Dizop Minoxidil Topical Gel1 in 1 CARTONGEL19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83766-101DIZOP MINOXIDIL TOPICAL GEL (MINOXIDIL 5%) GEL [SHENZHEN JOYUFLSH TECHNOLOGY CO.,LTD.]92 package rows20240425_089b2326-af24-9260-e063-6294a90a318d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83766-10183766-101-01, 83766-101-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
16cfe702-9dc8-dfce-e063-6294a90ab1db089b2326-af24-9260-e063-6294a90a318d2024-04-23WarningsExact identifier
spl id: 16cfe702-9dc8-dfce-e063-6294a90ab1db
spl set id: 089b2326-af24-9260-e063-6294a90a318d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.